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Completed

NCT Number: NCT02210390

Culturally Adapted Psychological Intervention for Bipolar Disorder in Pakistan

Aim:

To assess the Feasibility RCT of the efficacy of a culturally adapted psychological intervention for Bipolar disorder in Pakistan

Design:

Randomized Control Trial

Setting:

Psychiatric Departments of different Hospitals in Karachi.

Participants:

A total of 36 Bipolar disorder patients will be randomized to psychological Intervention and treatment as usual arm.

Intervention:

Culturally Adapted psychological intervention for bipolar disorder

Outcome measure:

* Acceptance of intervention in terms of attending session and dropouts * Knowledge and attitudes towards bipolar disorder

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Dow University of Health Sciences

Karachi, Sindh, Pakistan

About this study

The purpose of the study is to test Feasibility RCT of the efficacy of a culturally adapted psychological intervention for Bipolar disorder in Pakistan

Primary Objectives :

  • To determine effectiveness of educational intervention in terms of patient Satisfaction with overall care, knowledge and attitudes to bipolar disorder and medication adherence.
  • To assess feasibility in terms of
  • Recruitment
  • Using instruments that will be used to assess recurrence rate in the main study (BDI, YMRS and obtaining prospective hospitalisation and medication data)
  • acceptability of a culturally adapted bipolar group education package
  • To allow 'fine tuning' of culturally adapted bipolar group education package (this will partly be achieved by using the SEMI at study entry)

The Participants will be recruited from psychiatric department of different hospitals.

They will be randomly divided into two groups; intervention group and treatment-as-usual group. A total of thirty six participants will be recruited in the pilot study and divided equally into two arms. This will ensure that, even after loss to follow-up, we will have at least 12 subjects per group for analysis (FDA guidance http://www.fda.gov/cder/guidance/5356fnl.pdf) .Randomization will be carried out by the on offsite statistician. This will provide a reliable geographically remote service. For intervention group twelve sessions of psychoeducation will be provided by trained research clinician during the period of three months. Patients in the treatment as usual (TAU) group will be given details of intervention at the end of the study and interested patients will be offered psychoeducation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of DSM IV Bipolar disorder
  • Currently stable (YMRS <8, BDI<12)
  • Age 18 to 65 years.
  • Participants engaged with the mental health services since last 6 months.
  • Able to give written informed consent.
  • Resident of trial catchments area
  • Ability to speak Urdu /Punjabi

Exclusion criteria

  • Substance or alcohol dependent (i.e., those who fulfill the criteria for dependence according to DSM IV criteria)
  • Inability to engage fully in the psychotherapy (due to cognitive impairment)
  • Actively suicidal
  • Any major psychiatric illness other than bipolar disorder

Treatment and study plan

Psycho education

Behavioral

Psycho-education Sessions will be offered weekly basis

Primary outcomes

  1. Young Mania Rating Scale(YMRS)

    Time frame: three months

    The Young Mania Rating Scale (YMRS) is one of the most frequently utilized rating scales to assess manic symptoms

  2. Knowledge and attitudes

    Time frame: three months

    Knowledge and attitudes towards bipolar disorder measured by using a standard questionnaire

  3. Beck's Depression Inventory Scale (BDI)

    Time frame: three months

    The BDI is a measure of depression severity and has been used in several previous studies in Pakistan and is validated for use in Urdu.

Secondary outcomes

  1. Medication adherence

    Time frame: three months

    Self-reported Measure of Medication adherence

  2. Visual Analogue Scale

    Time frame: three months

    Patient satisfaction with overall care

  3. Short Explanatory Model Interview

    Time frame: three months

    used to elicit beliefs of mental illness

Sponsors and collaborators

Lead sponsor

Pakistan Institute of Living and Learning

Other

Collaborators

  • Abbasi Shaheed Hospital
  • Dow University of Health Sciences
  • University of Manchester

Registry information

Official study title

Feasibility RCT of the Efficacy of a Culturally Adapted Psychological Intervention for Bipolar Disorder in Pakistan

Important dates

Study start
2012
Primary completion
2015
Study completion
2015
First posted
Aug 6, 2014
Registry last updated
Dec 23, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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